PA-1 LOW PRESSURE ALARM

K Number: K802112 · Decision Sep 6, 1980

Classifications

FEI Numbers

Registration Numbers

Same Product Code

Applicant Total

110

Review Days

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K Number	Device Name	Decision Date	Decision
K063650	VENTILATOR WITH RESPIRATORY MECHANICS, MODEL 840	Feb 15, 2007	Substantially Equivalent
K053388	MODEL 840 VENTILATOR WITH PROPORTIONAL ASSIST VENTILATION PLUS SOFTWARE OPTION	Apr 4, 2006	Substantially Equivalent
K023225	PURITAN BENNETT DATAFLOW DATA MANAGEMENT SOFTWARE	Dec 18, 2002	Substantially Equivalent
K022103	PURITAN-BENNETT 700 RENAISSANCE II SPIROMETRY SYSTEM	Sep 27, 2002	Substantially Equivalent
K001646	PURITAN-BENNETT 840 VENTILATOR SYSTEM WITH NEOMODE OPTION	Oct 20, 2000	Substantially Equivalent - Subject to Tracking Reg.
K002001	BREEZE SLEEPGEAR WITH DREAMSEAL	Sep 6, 2000	Substantially Equivalent
K993071	PURITAN-BENNETT VENTILATOR SYSTEM WITH ET/TRACHEOSTOMY TUBE COMPENSATION, TC, OPTION, MODEL 840	Nov 24, 1999	Substantially Equivalent - Subject to Tracking Reg.
K993220	PURITAN-BENNETT HELIOS PORTABLE LIQUID OXYGEN SYSTEM	Oct 22, 1999	Substantially Equivalent
K993088	PURITAN-BENNETT AERIS 590 OXYGEN CONCENTRATOR WITH OCI	Oct 8, 1999	Substantially Equivalent
K984535	PURITAN-BENNETT 840 VENTILATORY SYSTEM WITH BILEVEL OPTION	Dec 28, 1998	Substantially Equivalent - Subject to Tracking Reg.

This FDA 510(k) entry is associated with 0 FEI numbers. Click on an entry to view related FDA registrations.

This FDA 510(k) entry is associated with 0 registration numbers. Click on an entry to view related FDA registrations.

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Applicant

Puritan Bennett Corp.

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